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Publikováno v:
Journal of Carbohydrate Chemistry. 36:100-110
An efficient and short stereoselective synthesis of C11–C19 fragment of Macrolactin 3 was achieved. The vic-triol moiety (C15–C17) was derived from the C2–C4 chiral centers of D-mannose. The C-1 of D-mannose was utilized for the Wittig-olefinat
Publikováno v:
Synthesis. 47:2997-3008
Stereoselective total synthesis of (+)-anamarine and the first synthesis of 8-epi-(–)-anamarine, its nonnatural diastereomer, were achieved from readily available d -mannitol. The key reactions involved were asymmetric dihydroxylation, cross-metath
Publikováno v:
Synthetic Communications. 45:1768-1776
Synthesis of two new amino acids, containing pyran rings, is reported from carbohydrate derivatives. The cis-3-amino-pyran-2-carboxylic acid (cis-APyC) was prepared from (R)-glyceraldehyde derivative, using nucleophilic substitution reaction for pyra
Publikováno v:
In Chemical Data Collections October 2021 35
Synthesis of two new amino acids, containing pyran rings, is reported from carbohydrate derivatives. The cis-3-amino-pyran-2-carboxylic acid (cis-APyC) was prepared from (R)-glyceraldehyde derivative, using nucleophilic substitution reaction for pyra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f7ac94c8faa5a7e1cafed7433b94ced